Rady Faculty of Health Sciences, University of Manitoba, GF324-820 Sherbrook Street, Winnipeg, Manitoba, R3A 1R9, Canada.
Seven Oaks General Hospital, Chronic Disease Innovation Centre, Winnipeg, Manitoba, Canada.
Osteoporos Int. 2020 Oct;31(10):1905-1912. doi: 10.1007/s00198-020-05458-1. Epub 2020 May 21.
Patients with chronic kidney disease have high risk of osteoporotic fractures. Lower trabecular bone score (TBS) was associated with poorer kidney function and higher fracture risk when kidney function was normal. Addition of TBS to The Fracture Risk Assessment Tool with bone mineral density did not improve fracture risk prediction.
We sought to determine whether trabecular bone score (TBS) either independently or adjusted for The Fracture Risk Assessment Tool (FRAX) could predict risk of major osteoporotic fractures (MOFs) in a large population-based sample of patients with all stages of chronic kidney disease (CKD).
We used population-based administrative databases to identify patients above age 20 years who had dual-energy X-ray absorptiometry (DXA) scan and serum creatinine measured within 1 year, during the years 2005 to 2010. Patients were excluded if they were on dialysis or had a functioning renal transplant. We stratified patients by estimated glomerular filtration rate (eGFR). We collected femoral neck bone mineral density (BMD), lumbar spine TBS, incident major osteoporotic fractures (MOF) and hip fractures, and other clinical characteristics.
Among 8289 patients, there were 6224 (75.1%) with eGFR ≥ 60 mL/min/1.73 m, 1624 (19.6%) with eGFR 30-60 mL/min/1.73 m, and 441 (5.3%) with eGFR < 30 mL/min/1.73 m. There were 593 patients (7.2%) with MOFs and 163 (2.0%) with hip fractures. Lower TBS score was associated with increased risk of MOF and hip fractures across all eGFR strata in unadjusted Cox proportional hazards models but after adjusting for FRAX with BMD, lower TBS was only statistically significant for MOF prediction for eGFR ≥ 60 mL/min/1.73 m.
Lower TBS scores were associated with lower eGFR and increased fracture risk in patients with eGFR ≥ 60 mL/min/1.73 m. However, the addition of TBS to the FRAX score with BMD did not significantly improve fracture risk prediction in patients with CKD.
慢性肾脏病患者骨质疏松性骨折风险较高。当肾功能正常时,较低的小梁骨评分(TBS)与肾功能较差和骨折风险增加相关。将 TBS 与骨密度的骨折风险评估工具(FRAX)联合使用并不能改善骨折风险预测。
我们旨在确定 TBS 无论是独立使用还是调整 FRAX 后,是否可以预测慢性肾脏病(CKD)各阶段患者的主要骨质疏松性骨折(MOF)风险。
我们使用基于人群的行政数据库,确定在 2005 年至 2010 年期间,年龄在 20 岁以上且在 1 年内进行过双能 X 射线吸收法(DXA)扫描和血清肌酐检测的患者。如果患者正在接受透析或进行了功能肾移植,则将其排除在外。我们按估计肾小球滤过率(eGFR)分层患者。我们收集了股骨颈骨密度(BMD)、腰椎 TBS、新发主要骨质疏松性骨折(MOF)和髋部骨折以及其他临床特征。
在 8289 名患者中,有 6224 名(75.1%)的 eGFR≥60mL/min/1.73m,1624 名(19.6%)的 eGFR 为 30-60mL/min/1.73m,441 名(5.3%)的 eGFR<30mL/min/1.73m。有 593 名(7.2%)患者发生 MOF,163 名(2.0%)患者发生髋部骨折。在未校正的 Cox 比例风险模型中,较低的 TBS 评分与所有 eGFR 分层中 MOF 和髋部骨折风险的增加相关,但在调整了 BMD 的 FRAX 后,仅在 eGFR≥60mL/min/1.73m 时,TBS 与 MOF 预测相关。
在 eGFR≥60mL/min/1.73m 的患者中,较低的 TBS 评分与较低的 eGFR 和骨折风险增加相关。然而,在 CKD 患者中,将 TBS 添加到 BMD 的 FRAX 评分中并未显著改善骨折风险预测。